Evidence map›Paper›PMID 38822328›Full record

ReviewVirology journal2024

The potential use of therapeutics and prophylactic mRNA vaccines in human papillomavirus (HPV).

Fatemeh Movahed, Satinik Darzi, Parya Mahdavi, Morug Salih Mahdi, Omer Qutaiba B Allela, Hayder Naji Sameer, Mohaned Adil, Hasna Zarkhah, Saman Yasamineh, Omid Gholizadeh

Abstract readReview
In one paragraph

Review in Virology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
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  7. Functional and therapeutic significant of heat-shock protein 90 (HSP90) in reproductive cancers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  8. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Fatemeh MovahedDepartment of Gynecology and Obstetrics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Satinik DarziDepartment Of Obstetrics and Gynecology, Abnormal Uterine Bleeding Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Parya MahdaviDepartment of Obstetrics and Gynecology, Faculty of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Morug Salih MahdiCollege of MLT, Ahl Al Bayt University, Karbala, Iraq.
Omer Qutaiba B AllelaDepartment of Pharmacy, Al-Noor University College, Nineveh, Iraq.
Hayder Naji SameerCollage of Pharmacy, National University of Science and Technology, Dhi Qar, 64001, Iraq.
Mohaned AdilPharmacy college, Al-Farahidi University, Baghdad, Iraq.
Hasna ZarkhahDepartment of Obstetrics and Gynaecology, Tabriz University of Medical Siences, Tabriz, Iran. hasnazarkhah@gmail.com.
Saman YasaminehYoung Researchers and Elite Club, Tabriz Branch, Islamic Azad University, Tabriz, Iran. Yassaman124@gmail.com.
Omid GholizadehAzad Researchers, Virology and Biotechnology, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer (CC) and other malignant malignancies are acknowledged to be primarily caused by persistent human papillomavirus (HPV) infection. Historically, vaccinations against viruses that produce neutralizing antibodies unique to the virus have been an affordable way to manage viral diseases. CC risk is decreased, but not eliminated, by HPV vaccinations. Since vaccinations have been made available globally, almost 90% of HPV infections have been successfully avoided. On the lesions and diseases that are already present, however, no discernible treatment benefit has been shown. As a result, therapeutic vaccines that elicit immune responses mediated by cells are necessary for the treatment of established infections and cancers. mRNA vaccines possess remarkable potential in combating viral diseases and malignancy as a result of their superior industrial production, safety, and efficacy. Furthermore, considering the expeditiousness of production, the mRNA vaccine exhibits promise as a therapeutic approach targeting HPV. Given that the HPV-encoded early proteins, including oncoproteins E6 and E7, are consistently present in HPV-related cancers and pre-cancerous lesions and have crucial functions in the progression and persistence of HPV-related diseases, they serve as ideal targets for therapeutic HPV vaccines. The action mechanism of HPV and HPV-related cancer mRNA vaccines, their recent advancements in clinical trials, and the potential for their therapeutic applications are highlighted in this study, which also offers a quick summary of the present state of mRNA vaccines. Lastly, we highlight a few difficulties with mRNA HPV vaccination clinical practice and provide our thoughts on further advancements in this quickly changing sector. It is expected that mRNA vaccines will soon be produced quickly for clinical HPV prevention and treatment.

Indexed as

mRNA VaccinesPapillomavirus InfectionsPapillomavirus VaccinesUterine Cervical NeoplasmsFemaleHuman Papillomavirus VirusesHumansOncogene Proteins, ViralPapillomaviridaeVaccines, SyntheticmRNA VaccinesOncogene Proteins, ViralPapillomavirus VaccinesVaccines, SyntheticmRNA vaccinesPapillomavirus (HPV)ProphylacticTherapeutic

Identifiers

PMID38822328
PMCPMC11143593

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.